CLASS I ONGOING Food recall · Reported 16 Mar 2022 · FDA Enforcement Report

Abbott Infant Formula Powder can recalled by Abbott Laboratories

Abbott Laboratories is recalling Abbott Infant Formula Powder can, distributed nationwide in the US. The recall was initiated on 17 Feb 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBatches: 29169K800
Quantity recalled500 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0957-2022
FDA event ID
89629
Recalling firm
Abbott Laboratories, Abbott Park, IL
Brand
Abbott
Classification
Class I
Status
Ongoing
Recall initiated
17 Feb 2022
FDA classified
30 Mar 2022
Reported
16 Mar 2022
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Salmonella
Product category
Baby Formula

Timeline

17 Feb 2022Recall initiated by company
16 Mar 2022Published in enforcement report+27 days
30 Mar 2022Classified by FDA+14 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Abbott Infant Formula Powder 12.6oz. can. 6 cans per case. Item numbers: Clinical Retail UPCs: N/A - Clinical

Where it was distributed

US Nationwide. Worldwide.

Nationwide

Questions about this recall

Is Abbott Infant Formula Powder can recalled?

Yes. Abbott Laboratories recalled Abbott Infant Formula Powder can on 17 Feb 2022. The recall is Class I and its status is Ongoing. Recall number F-0957-2022.

Why was it recalled?

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

Which lots are affected?

Batches: 29169K800

Where was it sold?

US Nationwide. Worldwide.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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